Open Access Article
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Correction: Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations

S. Hörner a, C. Uth a, O. Avrutina a, H. Frauendorf b, M. Wiessler c and H. Kolmar *a
aTechnische Universität Darmstadt, Clemens-Schöpf-Institut für Organische Chemie und Biochemie, Alarich-Weiss Straße 4, 64287 Darmstadt, Germany. E-mail: kolmar@biochemie-tud.de
bGeorg-August-Universität Göttingen, Institut für Organische und Biomolekulare Chemie, Zentrale Analytik/Massenspektrometrie, Tammannstraße 2, 37077 Göttingen, Germany
cDeutsches Krebsforschungszentrum, Medizinische Physik in der Radiologie, Projektgruppe Biologische Chemie E020, Im Neuenheimer Feld, 69120 Heidelberg, Germany

Received 23rd June 2015 , Accepted 23rd June 2015

First published on 30th June 2015


Abstract

Correction for ‘Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations’ by S. Hörner, et al., Chem. Commun., 2015, DOI: 10.1039/c5cc03434e.


In Fig. 1 of the published article the structures for compound 4 were displayed incorrectly. Fig. 1 should appear as follows:
image file: c5cc90302e-u1.tif

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


This journal is © The Royal Society of Chemistry 2015
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